Scientist I, QC Analytical(2nd Shift)
Tasks
- Analyze and interpret assay data
- Author and review GMP documents
- Conduct nucleic acid assays
- Conduct protein based assays
- Drive method optimization and validation
- Execute analytical methods
- Execute root cause investigations for OOS
- Implement CAPA
- Manage deviations and change controls
- Perform ELISA assays
- Perform cell based infectivity assays
- Perform in-process testing
- Perform lot release testing
- Perform potency assays
- Perform stability testing
- Perform viability assays
- Qualify analytical methods
- Review and approve GMP testing documentation
- Support GMP audits and inspections
- Track and trend testing data
- Troubleshoot assays
- Validate analytical methods
Perks/Benefits
- 401k match
- Employee assistance program
- Employee discounts
- Health, dental, and vision insurance
- Long-Term Disability coverage
- Mentorship programs
- Onsite fitness facility
- Paid time off
- Parental leave
- Professional development resources
- Short term disability coverage
Skills/Tech-stack
AUC | Analytical method execution | Assay Development | Assay validation | CAPA | CE | CGMP | Cause analysis | Cell based infectivity assays | Change Control | Data Analysis | DdPCR | Deviation Management | ELISA | EQMS | Infectivity assays | Informatics Systems | LIMS | Method qualification | Method validation | Nucleic acid extraction | OOS Investigation | Potency assays | Potency testing | QPCR | Root Cause Analysis | Root cause | Troubleshooting | Viability Assays
Education
Roles
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